Article
Lack of association between FXIII-Val34Leu, FVII-323 del/ins, and transforming growth factor beta1 (915G/T) gene polymorphisms and bronchopulmonary dysplasia: a single-center study.
DNA and cell biology - 1 Jan 2010
Ataç Fatma Belgin, Ince Deniz Anuk, Verdi Hasibe, Gökmen Zeynel, Yazici Ayse Canan, Gülcan Hande, Tarcan Aylin, Taneri Ayse, Sezgin Ezgi, Ozbek Namik
Abstract excerpt
Bronchopulmonary dysplasia (BPD) is a multifactorial disease of preterm infants that is characterized by airway injury, inflammation, and parenchymal remodeling. Extravascular fibrin deposits in septae and alveoli due to the altered fibrin turnover are the pathological hallmarks of BPD that strongly indicates the importance of the imbalance in the competing activities of coagulation and fibrinolysis. Activation...
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